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Results: 41 to 59 of 59

Tests names and labsConditionsGenes, analytes, and microbesMethods

Hyper/Hypokalemic Periodic Paralysis , Deletion-Duplications (MLPA) SCN4A Gene

Reference Laboratory Genetics
Spain
21
  • D Deletion/duplication analysis

Hyperkalemic Periodic Paralysis, Mutations (L6891, I693T, T704M, A1156T, M1360V, 1495F,M1592V, F1490L, M1493I) SCN4A Gene

Reference Laboratory Genetics
Spain
11
  • E Sequence analysis of select exons

Hyperkalemic Periodic Paralysis, Sequencing Exons (3,19,21-24) SCN4A Gene

Reference Laboratory Genetics
Spain
11
  • E Sequence analysis of select exons

Hyperkalemic Periodic Paralysis , Mutation (T704M) SCN4A Gene

Reference Laboratory Genetics
Spain
11
  • E Sequence analysis of select exons

Hyperkalemic Periodic Paralysis Type 2 , Sequencing SCN4A Gene

Reference Laboratory Genetics
Spain
11
  • C Sequence analysis of the entire coding region

Epilepsy Comprehensive NGS Panel

Fulgent Genetics
United States
729398
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Periodic paralysis Panel

CeGaT GmbH
Germany
45
  • C Sequence analysis of the entire coding region

Bartter Syndrome incl. differential diagnosis Panel

CeGaT GmbH
Germany
106
  • C Sequence analysis of the entire coding region

Single gene testing SCN4A

CeGaT GmbH
Germany
51
  • C Sequence analysis of the entire coding region

SCN4A Sequencing

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
51
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

SCN4A Single Gene

Fulgent Genetics
United States
61
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Congenital Myasthenic Syndrome NGS Panel

Fulgent Genetics
United States
10528
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51294672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Nuclear-Mito NGS Panel

Fulgent Genetics
United States
1103676
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hyperkalemic Periodic Paralysis

Molecular Genetics Laboratory BC Children's and BC Women's Hospitals
Canada
11
  • E Sequence analysis of select exons

Neuromuscular NGS Panel

Fulgent Genetics
United States
259112
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hyperkalemic periodic paralysis, type 2

MedGene
Slovakia
11
  • E Sequence analysis of select exons

Hyperkalemic periodic paralysis, type 2

Praxis fuer Humangenetik Wien
Austria
11
  • E Sequence analysis of select exons

Hyperkalemic Periodic Paralysis Type 1

MGZ Medical Genetics Center
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 41 to 59 of 59

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.